1999
DOI: 10.1155/s1110662x9900001x
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Photochemical and photobiological properties of furocoumarins and homologues drugs

Abstract: Abstract. Furocoumarins are natural photosensitizing drugs used in PUVA photochemotherapy and in photopheresis. Their therapeutic effectiveness is connected to the lesions they induce to various cell components, membranes, ribosomes, mitochondria, and in particular to DNA, damaged by formation of monofunctional adducts and of inter-strand cross-links (ISC). ISC represent a severe damage, mainly correlated to the main side effects observed in photochemotherapy, skin phototoxicity and genotoxicity. Searching for… Show more

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Cited by 19 publications
(3 citation statements)
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“…Ferulic acid and byakangelicin from A. dahurica inhibited Cladosporium herbarum growth, while (R)-heraclenol showed potent antibacterial activity against Bacillus subtilis [24]. These furocoumarins induce toxicity, mainly by causing abnormal DNA-protein interactions, or DNA inter-strand interactions [28]. The resistance of some microbes to these furocoumarins may be due to the presence of feruloyl catabolising enzymes [29].…”
Section: Angelica Speciesmentioning
confidence: 99%
“…Ferulic acid and byakangelicin from A. dahurica inhibited Cladosporium herbarum growth, while (R)-heraclenol showed potent antibacterial activity against Bacillus subtilis [24]. These furocoumarins induce toxicity, mainly by causing abnormal DNA-protein interactions, or DNA inter-strand interactions [28]. The resistance of some microbes to these furocoumarins may be due to the presence of feruloyl catabolising enzymes [29].…”
Section: Angelica Speciesmentioning
confidence: 99%
“…And, furanocoumarin-induced hepatotoxicity has been reported to occasionally occur in humans [7]. It was once believed that FCs could interact with proteins, lipids in membranes, Separations 2023, 10, 508 2 of 14 ribosomes, mitochondria, and, in particular, mono-and diadducts with DNA or RNA, which are the main contributors to toxicity in humans and animals [8][9][10]. In addition, certain FCs have been publicized to act as greatly potent inhibitors of a quantity of cytochromes P450 mono oxygenases [11], which can be interpreted as hepatotoxicity.…”
Section: Introductionmentioning
confidence: 99%
“…Psoralen has a greater tendency to form di-adducts than the methoxy analogues bergapten and xanthotoxin. Angelicin does not have a strong tendency to form di-adducts because of stearic hindrance (2)(3)(4)(5).…”
Section: Introductionmentioning
confidence: 99%